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. 2017 May 25;73(Pt 6):321–327. doi: 10.1107/S2053230X17006963

Table 1. Macromolecule-production information.

Source organism L. rhamnosus GG (ATCC 53103)
DNA source L. rhamnosus GG (ATCC 53103)
Forward primer 5′-CCACATTGGGTTCAGAATTCTGATCAAACTG
Reverse primer 5′-TGCGCCAATCGGACTCGAGCGGCAAATAAC
Cloning vector pET-28b(+) (Novagen)
Expression vector pET-28b(+) (Novagen)
Expression host E. coli BL21 (DE3) pLysS
Complete amino-acid sequence of the construct produced§ MGRDPNSDQTAEIVIHKRIYRDIRQPEDVWYENDGHRIDPNNPDKDGYKLLSKTSGLNGANFEVYDASSLLKPNMTPEAIRALVDRYQNMTRKQALKFARANLKLAGQGNKGIGLMNTKNDPTLGEDGISRITVSVDQQAPTKAYLMIEVAPDPSTELNVDLERKSSPMLVVFPVTDPISGNPLQTIHLYPKNVGYVRDPYFFKFGVHPDGTSKRLAGAIFAIYRIENGKKLYLDMSPVTDLRNKWVSTTDPLHDDRVNKFVSDQDGLVNTGERFLPAGEYFFEELQGVPGYEVDAKSRAIKIEIPDSWEDEDGNRRFVLIDGQPMQENFGGVVTPEMISSGYPRVYNYADKQASTTGDQTAGPSTTQLGNHGQDTNGTGTRTPKRQSGYLPLEHHHHHH

The EcoRI site is underlined.

The XhoI site is underlined.

§

The cloning artifacts are underlined.